The molecular basis of intellectual disability: novel genes with naturally occurring mutations causing altered gene expression in the brain.

Jozef Gécz
Published 2004 in
Frontiers in bioscience : a journal and virtual…

Abstract

This review on the genes implicated in mental retardation, and its X-chromosome linked forms, we presented at the symposium 'The Regulation of Gene Expression in the Brain' (January 23-26, 2003, Heron Island Australia). The main purpose of the review was to highlight the current knowledge of the spectrum of the genes causing mental retardation, provide an… (More)

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1 Figure or Table

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Cited By

X-linked mental retardation and epigenetics

Guy Froyen, Marijke Bauters, Thierry Voet, Peter Marynen
Journal of cellular and molecular medicine
2006

Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies.

Hyung-Goo Kim, Hyun-Taek Kim, +32 authors James F Gusella
American journal of human genetics
2012

Clinical and molecular characterization of overlapping interstitial Xp21-p22 duplications in two unrelated individuals.

Laura Thorson, Christine Bryke, +6 authors Gordana Raca
American journal of medical genetics. Part A
2010

Evolutionary genomics of human intellectual disability

Bernard Crespi, Kyle Summers, Steve Dorus
Evolutionary applications
2010

Mental retardation and Xq12-Xq23: candidate loci for nonspecific mental retardation in the male population of the QinBa region.

Kejin Zhang, Jing Zhang, +5 authors Fuchang Zhang
Psychiatric genetics
2009

Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.

Guy Froyen, Mark Corbett, +31 authors Jozef Gécz
American journal of human genetics
2008

Rho-linked genes and neurological disorders

Nael Nadif Kasri, Linda Van Aelst
Pflügers Archiv - European Journal of Physiology
2007

References

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Showing 1-10 of 63 references

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AGTR2 mutations in X-linked mental retardation.

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ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation.

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Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation.

A M Lossi, F Laugier-Anfossi, +7 authors L Villard
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Activity-dependent regulation of genes implicated in X-linked non-specific mental retardation.

B Boda, C Mas, D Muller
Neuroscience
2002

The molecular basis of intellectual disability: novel genes with naturally occurring mutations causing altered gene expression in the brain.

Abstract

Topics

1 Figure or Table

Cited By

X-linked mental retardation and epigenetics

Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies.

Clinical and molecular characterization of overlapping interstitial Xp21-p22 duplications in two unrelated individuals.

Evolutionary genomics of human intellectual disability

Mental retardation and Xq12-Xq23: candidate loci for nonspecific mental retardation in the male population of the QinBa region.

Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.

Rho-linked genes and neurological disorders

References

[Genetics of mental retardation].

Evolution of the human X - a smart and sexy chromosome that controls speciation and development

Induced gene expression in human brain after the split from chimpanzee.

Moraine: Non-syndromic X-linked mental retardation: where are the missing mutations

Mutations of the Xlinked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

A novel gene

AGTR2 mutations in X-linked mental retardation.

ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation.

Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation.

Activity-dependent regulation of genes implicated in X-linked non-specific mental retardation.

Slides referencing similar topics

The molecular basis of intellectual disability: novel genes with naturally occurring mutations causing altered gene expression in the brain.

Abstract

Topics

1 Figure or Table

Cited By

X-linked mental retardation and epigenetics

Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies.

Clinical and molecular characterization of overlapping interstitial Xp21-p22 duplications in two unrelated individuals.

Evolutionary genomics of human intellectual disability

Mental retardation and Xq12-Xq23: candidate loci for nonspecific mental retardation in the male population of the QinBa region.

Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.

Rho-linked genes and neurological disorders

References

[Genetics of mental retardation].

Evolution of the human X - a smart and sexy chromosome that controls speciation and development

Induced gene expression in human brain after the split from chimpanzee.

Moraine: Non-syndromic X-linked mental retardation: where are the missing mutations

Mutations of the Xlinked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

A novel gene

AGTR2 mutations in X-linked mental retardation.

ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation.

Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation.

Activity-dependent regulation of genes implicated in X-linked non-specific mental retardation.

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Slides referencing similar topics